Data suggest that all oral treatment regimen may have a role in the treatment of adolescent patients
April 16, 2016, Barcelona, Spain: Adolescents with Hepatitis C (HCV) could benefit from a combination of direct-acting antivirals, according to new data presented today at The International Liver Congress™ 2016 in Barcelona, Spain. The study demonstrated that adolescent patients with HCV genotype 1 aged 12 to 18 years who were treated for 12 weeks with a fixed dose combination of ledipasvir and sofosbuvir attained high sustained virologic response (SVR) rates.
Hepatitis C causes about 86,000 deaths per year in World Health Organization (WHO) European (EU) Region.1 Between 130 and 150 million people globally have chronic Hepatitis C infection,2 including approximately 15 million people in the EU.3 Children represent approximately 10% of those infected with the Hepatitis C virus (HCV), however some of these children have chronic disease and are at risk for complications. While direct-acting antivirals have been used to treat and cure almost all patients with HCV,4,5,6,7 they have been exclusively studied in adults, leaving adolescents to take pegylated interferon with ribavirin for 24 to 48 weeks.
“While there have been many studies investigating different treatment regimens for Hepatitis C in adults, data in adolescents have been lacking,” says study presenting author Dr Sanjay Bansal, Consultant Paediatric Hepatologist at King’s College Hospital, London and author of the study. “These data in HCV-infected adolescents confirm that this drug combination is effective in a younger population and has a more favourable side-effect profile than the treatments currently licensed for teenagers.”
The study included 100 patients aged between 12 and 18 years, infected with HCV genotype 1. In the open-label study, 100 patients received treatment with ledipasvir and sofosbuvir (90mg/400mg) once daily over a 12 week period. The primary efficacy endpoint was sustained viral response at 12 weeks post-treatment (SVR12).
Results from this study showed that of the 100 patients enrolled, 97% achieved SVR12 (n=97); the 3 patients who did not achieve SVR12 were lost to follow-up. No serious adverse events were reported, and the most common adverse events (reported by ≥10% of subjects) were headache (27%), diarrhoea (14%), fatigue (13%), nausea (12%), cough (10%) and vomiting (10%).
“These are very promising data for a patient group that has until now been excluded from the studies of newer agents in HCV infection,” said Professor Franck Tacke, Member of the EASL Governing Board. “We hope that this treatment regimen will provide these young patients with relief from this challenging condition.”
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About The International Liver Congress™
This annual congress is the biggest event in the EASL calendar, attracting scientific and medical experts from around the world to learn about the latest in liver research. Attending specialists present, share, debate and conclude on the latest science and research in hepatology, working to enhance the treatment and management of liver disease in clinical practice. This year, the congress is expected to attract approximately 10,000 delegates from all corners of the globe. The International Liver Congress™ takes place from April 13 – 17, 2016, at the Fira Barcelona Gran Via, Barcelona, Spain.
About EASL (www.easl.eu)
Since EASL’s foundation in 1966, this not-for-profit organisation has grown to over 4,000 members from all over the world, including many of the leading hepatologists in Europe and beyond. EASL is the leading liver association in Europe, having evolved into a major European Association with international influence, with an impressive track record in promoting research in liver disease, supporting wider education and promoting changes in European liver policy.
For more information, please contact the ILC Press Office at:
- Email: ILCpressoffice@ruderfinn.co.uk
- Telephone: +44 (0)7841 009 252
Onsite location reference
General session 3 and awards, Hall 6.0
Saturday 16 April, 08:30- 10:30
Presenter: Sanjay Bansal, United Kingdom
Abstract: GS17, High SVR rates of SVR12 in adolescents treated with the combination of ledipasvir/sofosbuvir
Author disclosures of interest
Clinical trials with Gilead, Roche, BMS, AbbVie, Novartis and Astellas.
1 World Health Organization. Hepatitis data and statistics. Available from: http://www.euro.who.int/en/health-topics/communicable-diseases/hepatitis/data-and-statistics. Last accessed: March 2016.
2 World Health Organization. Hepatitis C Fact Sheet N°164. Available from: http://www.who.int/mediacentre/factsheets/fs164/en/. Last accessed: March 2016.
3 World Health Organization. Global Alert and Response – Hepatitis C. Available from: http://www.who.int/csr/disease/hepatitis/whocdscsrlyo2003/en/index3.html. Last accessed: March 2016.
4 1 Afdhal N, et al. Ledipasvir and sofosbuvir for untreated HCV genotype 1 infection. N Engl J Med. 2014 May 15;370(20):1889-98.
5 Afdhal N, et al. Ledipasvir and sofosbuvir for previously treated HCV genotype 1 infection. N Engl J Med. 2014 Apr 17;370(16):1483-93.
6 Kowdley KV, et al. Ledipasvir and sofosbuvir for 8 or 12 weeks for chronic HCV without cirrhosis. N Engl J Med. 2014 May 15;370(20):1879-88.
7 Sulkowski MS, et al. Daclatasvir plus sofosbuvir for previously treated or untreated chronic HCV infection. N Engl J Med. 2014 Jan 16;370(3):211-21.